1Jalanko A, Braulke T. Neuronal ceroid lipofuscinoses[J]. Biochim Biophys Acta,2009,1793(4) :697 -709.
2Santavuori P. Neuronal ceroid-lipofuscinoses in childhood [J].Brain Dev, 1988,10 (2): 80-83.
3Alroy J ,Pfannl R,Ucci A,et al. Electron microscopic findings in skin biopsies from patients with infantile osteopetrosis and neuronal storage disease [J].Ultrastruct Pathol,2007,31(5):333-338.
4Goebel HH, Schochet SS, Jaynes M, et al. Progress in neuropathology of the neuronal ceroid lipofuseinoses[J]. Mol Genet Metab, 1999,66(4) :367-372.
1A. Simonati,N. Rizzuto. Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients[J] 2000,Neurological Sciences(1):S63～S70
2M. Villanova,C. Ceuterick,M. T. Dotti,F. M. Santorelli,C. Casali,A. Malandrini,N. De Stefano,U. Lübke,J. J. Martin,G. C. Guazzi,A. Federico. Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sj?gren)[J] 1999,Acta Neuropathologica(1):78～84
3Christiane Dumontel,Christophe Rousselle,M.-P. Guigard,J. Trouillas. Angulate lysosomes in skin biopsies of patients with degenerative neurological disorders: high frequency in neuronal ceroid lipofuscinosis[J] 1999,Acta Neuropathologica(1):91～96
4A. Gelot,C. A. Maurage,D. Rodriguez,D. Perrier-Pallisson,P. Larmande,M. M. Ruchoux. In vivo diagnosis of Kufs’ disease by extracerebral biopsies[J] 1998,Acta Neuropathologica(1):102～108
